• Research plot maintenance and preparation- Preparing sites to include planting, maintaining, spraying and harvesting the research plots. • Prepare for training sessions or grower field days. • Grooming plots and planning protocol execution to coincide with these events is paramount. • Crop scouting/advising - Walk research plots to evaluate weed control, insect infestations and disease outbreaks, consulting with Agronomists or Technical Seed Managers on solutions, and planning operations to resolve issues with crop production. • Help train and guide summer interns to complete operational goals. • Assist research manager with planning and organizing research activities.

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate • Demonstrates diligence in protecting the confidentiality of each subject/patient • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues • Assesses site processes and conducts Source Document Review of appropriate site source documents and medical records • Verifies required clinical data entered in the case report form (CRF) is accurate and complete • Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary • Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture • Verifies site compliance with electronic data capture requirements • May perform investigational product (IP) inventory, reconciliation and reviews storage and security • Prepares for and attends Investigator Meetings and/or sponsor face to face meetings.

Role Description Intetics is seeking a Research Assistant to CEO to act as an extension of the CEO, leveraging his social media presence and professional networks to drive business development. This role is not administrative support; it is a strategic and content-driven position for a highly capable, tech-savvy professional. - Maximize the CEO’s productivity by protecting and optimizing his time. - Conduct in-depth research on business and technology topics using Gen AI, online resources, and other tools. - Engage professionally with C-level executives and navigate corporate communications effectively. - Create high-quality written content: posts, articles, e-books, and more. - Manage and grow social media accounts, professional networks, and memberships. - Drive lead generation via social media and targeted content distribution. - Attend online conferences/webinars and deliver concise, insightful summaries. - Negotiate with service providers and coordinate relevant services. - Apply advanced social media expertise to enhance brand visibility. - Use modern Gen AI tools, including for avatar-based video production. - Perform basic web vibe coding tasks when needed. - Maintain meticulous attention to detail, even on repetitive tasks. Qualifications - Exceptional written and spoken English (C1+); German is a plus. - Strong analytical (IQ) and interpersonal (EQ) skills. - Proficiency in MS Office, including advanced PowerPoint skills. - Proven experience in social media management, business research, and professional communications. - Familiarity with AI tools for content creation and automation. - Ability to craft high-quality written content (posts, articles, reports) and communicate professionally with C-level executives. Flawless grammar, clarity, and tone are a must. - Proven experience supporting executive leadership (3+ years). - Demonstrated ability to proactively manage and protect the time, priorities, and communications of a CEO or other top executive. - Hands-on expertise with Gen AI tools. - Confident use of modern AI solutions for content creation, research, automation, and avatar-based video production. Curiosity and adaptability in experimenting with new tools. - Strong digital and social media skills. - Experience managing and growing personal or brand profiles (LinkedIn, X/Twitter, etc.), creating targeted content, and driving lead generation through social channels. - High autonomy, reliability, and attention to detail. - Ability to operate independently, handle a wide range of tasks without supervision, and maintain high-quality output — even with repetitive or complex assignments. - Excellent research and analytical skills. - Capacity to quickly absorb and synthesize complex business and tech topics, summarize key insights, and support strategic decision-making. Benefits - A strategic role in a reputable, globally recognized company. - Opportunity for self-expression, innovation, and real impact. - Competitive compensation with profit sharing. - Collaborative, mission‑driven organizational culture.

• Independently oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. • Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions. • Establishes, updates, tracks and maintains study specific trial management tools/systems, and status reports. • Manages site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager. • If required, assists the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee. • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. • Independently conducts all forms of site visits, including pre-study/qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs. Performs Monitoring Oversight Visits to assess other CRA team members. Prepares and submits for review, accurate and timely monitoring reports from all site visits (on-site and remote).